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Is one diagnosis the whole story? patients with double diagnoses.
Kurolap, Alina; Orenstein, Naama; Kedar, Inbal; Weisz Hubshman, Monika; Tiosano, Dov; Mory, Adi; Levi, Zohar; Marom, Daphna; Cohen, Lior; Ekhilevich, Nina; Douglas, Jessica; Nowak, Catherine Bearce; Tan, Wen-Hann; Baris, Hagit N.
Afiliação
  • Kurolap A; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
  • Orenstein N; The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Institute of Technology, Haifa, Israel.
  • Kedar I; Genetics Unit, Schneider Children Medical Center, Petach Tikva, Israel.
  • Weisz Hubshman M; The Raphael Recanati Genetics Institute, Rabin Medical Center, Beilinson Hospital, Petach Tikva, Israel.
  • Tiosano D; Genetics Unit, Schneider Children Medical Center, Petach Tikva, Israel.
  • Mory A; The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Institute of Technology, Haifa, Israel.
  • Levi Z; Pediatric Endocrinology, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, Haifa, Israel.
  • Marom D; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
  • Cohen L; The Early Detection and High Risk GI Cancer Service, Gastroenterology Division, Rabin Medical Center, Petach Tikva, Israel.
  • Ekhilevich N; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Douglas J; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Nowak CB; Pediatric A, Schneider Children Medical Center, Petach Tikva, Israel.
  • Tan WH; The Raphael Recanati Genetics Institute, Rabin Medical Center, Beilinson Hospital, Petach Tikva, Israel.
  • Baris HN; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
Am J Med Genet A ; 170(9): 2338-48, 2016 09.
Article em En | MEDLINE | ID: mdl-27271787
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudos de Associação Genética / Doenças Genéticas Inatas Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudos de Associação Genética / Doenças Genéticas Inatas Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Ano de publicação: 2016 Tipo de documento: Article